DOSI-FUSER

Pump, Infusion, Elastomeric

LEVENTON, S.A.

The following data is part of a premarket notification filed by Leventon, S.a. with the FDA for Dosi-fuser.

Pre-market Notification Details

Device IDK040752
510k NumberK040752
Device Name:DOSI-FUSER
ClassificationPump, Infusion, Elastomeric
Applicant LEVENTON, S.A. C/NEWTON 18-24, POLIGONO INDUSTRIAL SESROVIRES, SANT Esteve Sesrovires, Barcelona,  ES 08635
ContactJoaquim Soriano
CorrespondentStefan Priss
TUV AMERICA, INC. 1775 OLD HIGHWAY 8 New Brighton,  MN  55112 -1891
Product CodeMEB  
CFR Regulation Number880.5725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedYes
Combination ProductNo
Date Received2004-03-24
Decision Date2004-04-07
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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18436020760010 K040752 000

Trademark Results [DOSI-FUSER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DOSI-FUSER
DOSI-FUSER
79107543 4273860 Live/Registered
LEVENTON S.A.
2011-12-02

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